General Information
The MDS 2025 General Information page has all the important information conveniently collected in one place. If you have any further questions that we have left answered, do not hesitate to contact us.
De Doelen ICC Rotterdam
Schouwburgplein 50, 3012 CL Rotterdam, Netherlands
Google Maps: https://maps.app.goo.gl/Ndc9ou6Ce7caRk4u5
The International Congress will officially run on Central European Summer Time (CEST) / (GMT+2).
The official language of the International Congress will be English. All abstract submissions and presentations should be in English.
An official personalized letter of invitation will be provided to registered participants as part of the registration procedure. This invitation is prepared solely for the purpose of visa applications and is not a commitment on the part of the organizers to provide any financial support or confirmation of inclusion in the Scientific Program.
Participants are advised to wear business casual for all International Congress functions and programs.
All event activities (including educational sessions, meal functions, exhibit hall, etc.) are exclusively reserved for registered attendees. Non-registered guests (including children, family members, colleagues, etc.) are not allowed in any of the event areas. Badges provided at registration are required for entrance into all functions and will be strictly enforced.
Please do not leave bags or suitcases unattended at any time, whether inside or outside the session halls. Hotels strongly recommend that you use their safety deposit boxes for your valuables.
The Congress Secretariat and Organizers cannot accept liability for personal accidents or loss of or damage to private property of participants. Participants are advised to take out their own personal travel and health insurance for their trip.
An exhibition will be held. See the Sponsorship & Exhibition page, for more details regarding support, and if you have any questions, please reach out by clicking here.
Support from pharmaceutical partners helps make this event possible. As such, it is important that we comply with the various codes and directives relating to the manufacturing, distribution, and marketing of pharmaceutical products. The European Union directive (2001/83/EC, article 86) provides guidelines relating to medicinal products for human use. Within these guidelines is the restriction that access to pharmaceutical product marketing activities must be limited to only those participants licensed/authorized to prescribe or supply medicinal products. All participants, with the exception of the exhibitors, are asked the following question during registration: Are you licensed/authorized to prescribe or supply prescription-only medicines?
If you have any questions, please be sure to check out our Frequently Asked Questions or send us an email via the Contact Us form.